These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
79 related articles for article (PubMed ID: 3434474)
1. About changes of the phenylalanine-tyrosine metabolism in psoriasis vulgaris. Knapp A Acta Univ Carol Med (Praha); 1986; 32(3-4):203-6. PubMed ID: 3434474 [No Abstract] [Full Text] [Related]
3. [Method of detection of heterozygotic carrier state in phenylketonuria]. Baikov AD; Sitnichenko EI Lab Delo; 1973; 5():293-5. PubMed ID: 4129158 [No Abstract] [Full Text] [Related]
4. [Detection of heterozygotes of typical phenylketonuria]. Farriaux JP; Delabre M Arch Fr Pediatr; 1972 Apr; 29(4):365-72. PubMed ID: 5053206 [No Abstract] [Full Text] [Related]
5. [In vitro synthesis of tyrosine from phenylalanine in human platelets]. Uebelhack R; Franke L; Kutter D; Thoma J; Seidel K Biomed Biochim Acta; 1984; 43(7):1037-9. PubMed ID: 6517886 [No Abstract] [Full Text] [Related]
6. [Intravenous phenylalanine loading test in normal subjects and the parents of phenylketonuretics]. Badinand A; François R; Site J; Quincy C; Mamelle N; Masson E; Later R C R Seances Soc Biol Fil; 1968; 162(8):1525-8. PubMed ID: 4238174 [No Abstract] [Full Text] [Related]
7. [Rapid high performance liquid chromatography for determination of phenylalanine and tyrosine in serum]. Tang AG Hunan Yi Ke Da Xue Xue Bao; 2000 Apr; 25(2):209-12. PubMed ID: 12212229 [TBL] [Abstract][Full Text] [Related]
8. [Phenylalanine-tyrosine metabolism in psoriasis vulgaris. Search on a genetic basic defect (author's transl)]. Knapp A; Grimm U; Postrach E Dermatol Monatsschr; 1980 Jul; 166(7):470-7. PubMed ID: 7428990 [No Abstract] [Full Text] [Related]
9. [A new method of detection of heterozygotes in phenylpyruvic oligophrenia]. Mamelle N; Mamelle JC; Site J; Quincy C; Later R; Masson E; Moreau P; François R Rev Eur Etud Clin Biol; 1971 Apr; 16(4):342-51. PubMed ID: 5564546 [No Abstract] [Full Text] [Related]
10. Use of aspartame in phenylketonuric heteroxygous adults. Koch R; Shaw KN; Williamson M; Haber M J Toxicol Environ Health; 1976 Nov; 2(2):453-7. PubMed ID: 796477 [TBL] [Abstract][Full Text] [Related]
11. Discriminant analysis for detection of phenylketonuric heterozygotes. Christian BG Soc Biol; 1971 Mar; 18(1):64-72. PubMed ID: 5580588 [No Abstract] [Full Text] [Related]
12. Detection of phenylketonuric heterozygotes. Jackson SH; Hanley WB; Gero T; Gosse GD Clin Chem; 1971 Jun; 17(6):538-43. PubMed ID: 5103385 [No Abstract] [Full Text] [Related]
13. Biochemical phenotype and its relationship with genotype in hyperphenylalaninemia heterozygotes. Mallolas J; Milà M; Lambruschini N; Cambra FJ; Campistol J; Vilaseca MA Mol Genet Metab; 1999 Jun; 67(2):156-61. PubMed ID: 10356315 [TBL] [Abstract][Full Text] [Related]
14. Intracellular concentrations of phenylalanine, tyrosine and alpha-aminobutyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria (PKU) compared with 26 normals. Thalhammer O; Pollak A; Lubec G; Königshofer H Hum Genet; 1980; 54(2):213-6. PubMed ID: 7390492 [No Abstract] [Full Text] [Related]
15. Intracellular concentrations of phenylalanine, tyrosine and alpha-aminobutyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria compared with 26 normals. Thalhammer O; Pollak A; Lubec G; Königshofer H J Inherit Metab Dis; 1981; 4(2):73-4. PubMed ID: 6790854 [No Abstract] [Full Text] [Related]
16. Detection of phenylketonuria carriers. Kelly S; Rose F Public Health Rep (1896); 1969 Feb; 84(2):144-8. PubMed ID: 4980161 [No Abstract] [Full Text] [Related]
17. [Heterozygote identification in phenylketonuria]. Rampini S; Anders PW; Curtius HC; Marthaler T Arch Julius Klaus Stift Vererbungsforsch Sozialanthropol Rassenhyg; 1968; 43(3-4):suppl 102-3. PubMed ID: 5761621 [No Abstract] [Full Text] [Related]
18. Detection of heterozygotes for phenylketonuria. Total body phenylalanine clearance and concentrations of phenylalanine and tyrosine in the plasms of fasting subjects compared. Jagenburg R; Regårdh CG; Rödjer S Clin Chem; 1977 Sep; 23(9):1654-60. PubMed ID: 890909 [TBL] [Abstract][Full Text] [Related]
19. Phenylketonuria: a family study. Crosby PF; Navarro A; Matos ML Bol Asoc Med P R; 1969 Apr; 61(4):133-7. PubMed ID: 5255738 [No Abstract] [Full Text] [Related]
20. Mental retardation in a family with phenylketonuria and mild hyperphenylalaninemia. Cohen BE; Szeinberg A; Berman W; Aviad Y; Crispin M; Hirshorn N; Goland R Pediatrics; 1969 Nov; 44(5):655-60. PubMed ID: 5374976 [No Abstract] [Full Text] [Related] [Next] [New Search]